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RECRUITING
NCT05880381
NA

Virtual Reality for Coping With Involuntary Early Pregnancy Loss

Sponsor: Universidade da Madeira

View on ClinicalTrials.gov

Summary

This study aims to provide psychological support to women that experienced an Early Pregnancy Loss (when the loss occurs until the 20 weeks of gestation) using an innovative Virtual Reality prototype and compare the presence and evolution of psychological distress symptoms pre and post-intervention. The main goals of this study are: 1. Evaluate the impact of the proposed VR paradigm in women who suffered a gestational loss in the first 20 weeks of gestation, compared to a control group that follows the usual standard care; 2. Evaluate the usability, user experience, and acceptance of the proposed approach. Participants in the VR group will have an intervention program lasting four weeks, with 3 weekly sessions of 45-60 minutes, using the developed prototype.

Official title: Adaptive Virtual Reality for Coping With Involuntary Early Pregnancy Loss

Key Details

Gender

FEMALE

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

20

Start Date

2023-05-01

Completion Date

2025-09-30

Last Updated

2025-03-25

Healthy Volunteers

Yes

Interventions

DEVICE

Virtual Reality Group

Patients allocated to the treatment group will undergo an intervention that comprises 3 weekly sessions of 60 minutes for 4 weeks with the VR prototype.

OTHER

Control Group

The participants allocated to this group will do the formal standard care provided by the Gynecology- Obstetric service.

Locations (1)

Universidade da Madeira

Funchal, Portugal